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Our clinical trial portfolio is one of the largest in the country. We have more than 700 clinical trials open across 30 clinical units.

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627 clinical trials found
Clinical trials

SYNOVIIIUS

Prospective Interventional Study of Effectiveness of Efanesoctocog Alfa Prophylaxis on Synovial Hypertrophy in Patients with Hemophilia A (NCT06941870)

This study will use MRI and Ultrasound techniques to help track the health of joints in patients with Haemophilia A taking Efanesoctocog Alfa Prophylaxis. The study will take place over the course of 1 year and will involve up to 5 outpatient visits (plus scans). The Efanesoctocog Alfa will be taken at home via IV (patients/guardians will be trained prior).
Coming soon

TACTI-004

TACTI-004, a double-blinded, randomized phase 3 trial in patients with advanced/metastatic non-small cell lung cancer [NSCLC] receiving eftilagimod alfa [MHC class II agonist] in combination with pembrolizumab [PD-1 antagonist] and chemotherapy.

The purpose of this study is to compare eftilagimod alfa (efti) in combination with pembrolizumab and chemotherapy versus placebo in combination with pembrolizumab and chemotherapy among adults with metastatic non-small cell lung cancer (NSCLC).
Currently recruiting

TAK-079-3003

A Phase 3, Open-label, Multicenter Continuation Trial to Evaluate the Long-term Safety and Efficacy of Mezagitamab Subcutaneous Injection in Adults with Chronic Primary Immune Thrombocytopenia (NCT06948318)

A continuation study for patients rolling over from TAK-079-3002 or TAK-079-1004 with the purpose of evaluating the long-term efficacy of mezagitamab in participants ?18 years of age with chronic primary ITP. The trial is structured to include periods of safety follow up, long term observation and on-demand dosing.

Coming soon

TAK-279

A Phase 2, Multicenter, Randomized, Placebo-Controlled, Double-Blind Induction Study to Evaluate the Efficacy and Safety of Oral TAK-279 in Subjects with Moderately to Severely Active Ulcerative Colitis (NCT06254950)

The main aim of this study is to learn if TAK-279 reduces bowel inflammation and symptoms compared to placebo. Another aim is to compare any medical problems that participants have when they take TAK-279 or placebo and how well the participants tolerate any problems.

The participants will take capsules of either TAK-279 or placebo for up to 3 months (12 weeks). Then all the participants will receive TAK-279 for the rest of the treatment part of the study (1 year or 52 weeks).

During the study, participants will visit their study clinic several times.

Currently recruiting

TAK-279-HS-2001

A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial to Assess Efficacy and Safety of Zasocitinib in Moderate to Severe Hidradenitis Suppurativa (NCT07244263)

This trial aims to evaluate the safety and efficacy of zasocitinib vs. Placebo in adults with Hidradenitis Suppurativa (HS). The participants will receive the study treatment (either zasocitinib or placebo) for up to 4 months (16 weeks). The placebo looks like the zasocitinib capsule but does not have any medicine in it. After the first 4 months, all participants (also those who initially received placebo) will then receive zasocitinib for up to 8 months (36 weeks). During the study, participants will visit their study clinic 12 times. 

Coming soon

Targeting peripheral airways in asthma

Targeting peripheral airway dysfunction with small particle bronchodilator in asthma

This study aims to determine whether the small airways, a site of physiological dysfunction in asthma, can be targeted with bronchodilator therapy, by using a small particle size aerosol that reaches the lung periphery. Current clinical management of patients with asthma includes an array of inhaled therapies. However, there is no consensus relating to the efficacy of different particle sizes for inhalation, despite particle size being the main determinant of where the drug deposits in the airway. Participants with asthma will be invited to participate in two study visits. Both study visits will involve physiological assessments (lung function tests) and ventilation scans completed at baseline and post-bronchodilator. At one visit the standard medication salbutamol will be administered via a conventional vibrating mesh nebuliser (Aerogen solo), at the other visit the salbutamol will be administered via the Aerogen PDAP which will create a fine particle aerosol. The aim is 2 recruit and test 30 participants and compare their response to small and large particle bronchodilator.
Currently recruiting